Breast Cancer Clinical Trial

A Pilot Trial to Assess the Impact of Acupuncture on Post-mastectomy Pain, Nausea, Anxiety and Ability to Cope

Summary

The purpose of the study is to compare the effect of acupuncture to the standard of care (control group) on pain, nausea, anxiety, ability to cope, costs and length of hospital stay in post-mastectomy patients at Abbott Northwestern Hospital.

View Full Description

Full Description

About 40 subjects will be participating in this study. Following qualification for the study, participants will be randomly assigned by chance to receive either acupuncture or to receive the standard of care without an integrative medicine session.

One group will receive acupuncture after surgery. Acupuncture involves inserting thin, sterile needles at certain points on your body.
The other group will receive the standard of care without an acupuncture session.

Before surgery participants will complete a demographics questionnaire. After surgery, participants will be visited in their hospital room by either an acupuncturist or another member of the research team. For those assigned to the acupuncture group, participants will receive up to two sessions of acupuncture, at least twelve hours apart. For those assigned to the control group, a research team member will visit the participant in their room up to two times, at least twelve hours apart. During those visits, participants will be asked about pain, nausea, anxiety, and ability to cope at the beginning and end of each treatment or visit.

Additional information will be gathered from participants hospital charts, such as the type of surgery that was performed, length of hospital stay, and the costs associated with the hospital stay.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Women
18 years or older
Undergoing mastectomy surgery

Exclusion Criteria:

Non-English speaking
Pregnant
Also undergoing an oophorectomy, TRAM or Latissimus flap surgery

Study is for people with:

Breast Cancer

Estimated Enrollment:

30

Study ID:

NCT02122796

Recruitment Status:

Completed

Sponsor:

Allina Health System

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

Abbott Northwestern Hospital
Minneapolis Minnesota, 55407, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

30

Study ID:

NCT02122796

Recruitment Status:

Completed

Sponsor:


Allina Health System

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider